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4-MEO-C6H4-SIME3
SpectraBase Compound ID 2Fqc12PxCkj
InChI InChI=1S/C10H16O2Si/c1-11-9-5-7-10(8-6-9)12-13(2,3)4/h5-8H,1-4H3
InChIKey TXFCNWLJGZXMHT-UHFFFAOYSA-N
Mol Weight 196.32 g/mol
Molecular Formula C10H16O2Si
Exact Mass 196.091956 g/mol
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Biologically and Environmentally Important Organic Compounds: GCMS Library
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-20-616-6
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O5-0-487-0
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • TRIMETHYL-(4-METHOXYPHENOXY)-SILANE
  • Silane, (4-methoxyphenoxy)trimethyl-
  • Anisol <4-hydroxy->, mono-TMS
  • 4-Hydroxyanisol, mono-TMS
Title Journal or Book Year
The effect of solvent accessible surface on Hammett‐type dependencies of infinite dilution 29Si and 13C NMR shifts in ring substituted silylated phenols dissolved in chloroform and acetone Magnetic Resonance in Chemistry 2012
29Si–13C spin–spin couplings over Si–O–Carom link Magnetic Resonance in Chemistry 2006

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